1-Bromo-3-chloropropane → 4-(3-Chloropropyl)morpholine
Reaction equation
[NH:1]1[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1.Br[CH2:8][CH2:9][CH2:10][Cl:11]>C1(C)C=CC=CC=1>[Cl:11][CH2:10][CH2:9][CH2:8][N:1]1[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of morpholine (261 ml, 3.00 mol) and 1-bromo-3-chloropropane (148 ml, 1.50 mol) in toluene (900 ml) was stirred for 18 hours at ambient temperature. Additional 1-bromo-3-chloropropane (25 ml, 0.25 mol) was added, the reaction was stirred for a further 1 hour and then filtered to remove the precipitated solid before the filtrate was concentrated in vacuo. Distillation of the crude oil yielded N-(3-chloropropyl)-morpholine (119.3 g, 49% yield) as the fraction boiling at 70–80° C./2.6 mmHg:
Workup
- stirringthe reaction was stirred for a further 1 hour
- filtrationfiltered
- customto remove the precipitated solid before the filtrate
- concentrationwas concentrated in vacuo
- distillationDistillation of the crude oil
Sources & evidence
- ORD record
- ord-6769e4d70b70423bb3e2cddc878aa34a
- Source dataset
- uspto-grants-2007_06
- Patent number
- US07235559B1
Reaction notes
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